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hal.structure.identifierBioinorganic Laboratory, Department of Chemistry
dc.contributor.authorALI, Amjad
hal.structure.identifierBioinorganic Laboratory, Department of Chemistry
dc.contributor.authorRAO, Chebrolu P.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorGUIONNEAU, Philippe
dc.date.issued2008
dc.identifier.issn0370-0089
dc.description.abstractEnRole of alkali and alkaline earth ions on the formation of calix[4]arene-amide derivatives through O-alkylation of the lower rim phenolic-OH groups in general and template action of K+ in particular have been explored. Na+ and K+ ions among alkali, and Ca2+ and Sr2+ ions among alkaline earth have shown tetra-amide derivatives bound to metal ion species. Among all these, potassium salts act as template and yields a K+ bound tetra-amide derivative where the charge is counter balanced by a calix[4] arene-monoanion and the product is crystallographically characterized. Change in the amide precursor used in these O-alkylation reactions has no effect on the type of the amide derivative formed. Also demonstrated is a direct one-step reaction for the preparation of 1,3-di-amide derivative in high yield and low reaction period using CsHCO3.
dc.language.isoen
dc.publisherIndian Academy of Sciences
dc.subject.enO-alkylation at the lower rim of calix[4]arene
dc.subject.enTemplate action of K+
dc.subject.enMono-anion of p-tert-butyl-calix[4]arene
dc.subject.enAlkali and alkaline earth ions
dc.title.enInfluence of alkali and alkaline earth ions on the O-alkylation of the lower rim phenolic-OH groups of p-tert -butyl-calix[4]arene to result in amide-pendants: Template action of K+ and the structure of K+ bound tetra-amide derivative crystallized with a p-tert -butyl-calix[4]arene anion
dc.typeArticle de revue
dc.identifier.doi10.1007/s12039-008-0029-9
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Chemical Sciences
bordeaux.page237-247
bordeaux.volume120
bordeaux.issue2
bordeaux.peerReviewedoui
hal.identifierhal-00277240
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00277240v1
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